具有丰富氧空位的多界面纳米片-互鳞片结构促进电催化氧进化

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL Catalysis Science & Technology Pub Date : 2024-09-16 DOI:10.1039/d4cy00653d
Di Wang , Zhe Sun , Wenguang Cui , Chaozhen He , Zhongkui Zhao
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引用次数: 0

摘要

界面上的电子耦合效应和氧空位(Ov)的引入对电催化活性起着至关重要的作用。降低氧进化反应(OER)能量势垒的关键在于正确构建界面和增加氧空位。在这项研究中,通过水热法和电化学氧化法这两个简单的步骤,在泡沫镍上制备出了一种具有丰富氧空位和多界面纳米片插层结构的磷化镍催化剂,命名为 (Fe,La)Ni2P-r。Fe-La 的加入在催化剂表面形成了一个异质界面,导致电子转移和再分布,并降低了中间产物的结合能。同时,结合 DFT 发现,Fe-Ov-La 的加入大大降低了反应过程的吉布斯自由能,增强了中间产物的吸附,加速了氧气的释放。电流密度为 10 mA cm-2 时仅需 197 mV,法拉第效率约为 100%,电流密度为 800 mA cm-2 时所需电压为 390 mV。这项研究不仅提出了一种出色的富氧多界面 OER 电催化剂,还为开发具有成本效益的贵金属和多金属催化剂铺平了道路。
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Multi-interfacial nanosheet-intercalated structure with abundant oxygen vacancies promotes electrocatalytic oxygen evolution†
The electron coupling effect at the interface and the introduction of oxygen vacancies (Ov) play critical roles in the electrocatalytic activity. The key to lowering the energy barrier of the oxygen evolution reaction (OER) is to build the interface properly and increase oxygen vacancies. In this work, a nickel phosphide on nickel foam-derived catalyst with rich Ov and a multi-interfacial nanosheet intercalated structure, labeled as (Fe,La)Ni2P-r, was created on nickel foam by using a straightforward two-step technique, namely hydrothermal and electrochemical oxidation. The addition of Fe–La creates a heterogeneous interface on the catalyst surface, causes electron transfer and redistribution, and lowers the binding energy of intermediates. At the same time, connected with DFT, it was discovered that the addition of Fe–Ov–La significantly lowered the Gibbs free energy of the reaction process, enhanced the intermediate species adsorption, and hastened the oxygen release. Only 197 mV was required to obtain a current density of 10 mA cm−2 with a Faraday efficiency of around 100%, and the required voltage is 390 mV at a current density of 800 mA cm−2. This study not only presents an excellent Ov-enriched multi-interface OER electrocatalyst, but also paves a path for the development of cost-effective noble metal and polymetallic catalysts.
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
期刊最新文献
Back cover Back cover Insight into the influence of Re and Cl on Ag catalysts in ethylene epoxidation. Back cover Improved charge carrier mobility in a copper oxide heterostructure enhances the photocatalytic partial oxidation of benzyl alcohol to benzaldehyde†
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